Biologically Oriented Alveolar Ridge Preservation (BARP) With and Without Advanced Platelet-Rich Fibrin Plus (A-PRF+)
Comparative Evaluation of Biologically Oriented Alveolar Ridge Preservation (BARP) With and Without Advanced Platelet-Rich Fibrin Plus (A-PRF+) For Delayed Implant Placement in Maxillary Premolars
1 other identifier
interventional
20
1 country
1
Brief Summary
Twenty patients were selected from the outpatient clinic of the Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Mansoura University seeking for extraction of non-restorable maxillary premolar teeth prior to delayed implant placement. Patients will be divided into 2 groups:
- Group A: 10 implants were inserted after four months from extraction after socket preservation by putting two collagen sponge layers and in between deproteinized bovine bone.
- Group B: 10 implants were inserted after four months after socket preservation by putting two collagen sponge and in between deproteinized bovine bone with addition of advanced PRF plus layer.
- Closure of the flap was obtained without tension. Implants of all groups were immediately loaded .Some Clinical and Radiographic parameters and Histological and Volumetric evaluation were made at different time intervals along this study.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Nov 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 7, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
September 8, 2026
CompletedFirst Submitted
Initial submission to the registry
October 4, 2026
CompletedFirst Posted
Study publicly available on registry
October 9, 2026
CompletedOctober 9, 2026
October 1, 2026
5 months
October 4, 2026
October 6, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Implant stability
Implant stability measured using Resonance Frequency Analysis (RFA) with the Osstell Mentor device and SmartPeg. Measurements were recorded in four directions (every 90 degrees) and averaged per implant to provide an ISQ score (scale: 1 to 100, where higher scores indicate greater stability).
6 months
Study Arms (2)
Deproteinized bovine
EXPERIMENTALDeproteinized bovine bone with collagen sponge was used for socket preservation for 10 cases and implant placement was performed after four months.
Deproteinized bovine bone with advanced PRF
EXPERIMENTALDeproteinized bovine bone with advanced PRF+ and collagen sponge was used for socket preservation for 10 cases then implant placement was performed after four months.
Interventions
After atraumatic extraction, socket preservation by deproteinized bovine bone and collagen sponge was done and implant placement was performed after four months from that.
After atraumatic extraction, socket preservation by deproteinized bovine bone mixed with advanced PRF+ and collagen sponge was done and implant placement was performed after four months from that.
Eligibility Criteria
You may qualify if:
- Patient with good oral hygiene.
- Age (18-50) years.
- Presence of non-restorable maxillary premolar teeth due to caries, root resorption, roots fracture, etc.
- No history of parafunctional habits
- Adequate inter arch space
- Patients prepared to comply with the follow-up and maintenance program.
You may not qualify if:
- Patients with systemic diseases that interfere with dental implant insertion.
- Smokers.
- Pregnancy.
- Immunocompromised patients.
- Presence of acute infection at the tooth to be extracted
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of Dentistry Mansoura University
Al Mansurah, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 4, 2026
First Posted
October 9, 2026
Study Start
November 1, 2025
Primary Completion
April 7, 2026
Study Completion
September 8, 2026
Last Updated
October 9, 2026
Record last verified: 2026-10